Evidence map›Paper›PMID 30645749›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2019

Serum orexin-A levels are associated with disease progression and motor impairment in multiple sclerosis.

Mehmet Gencer, Ece Akbayır, Melis Şen, Erdil Arsoy, Vuslat Yılmaz, Nesrin Bulut, Erdem Tüzün, Recai Türkoğlu

Abstract read
PubMed Publisher
In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Observational
  3. Sexual dysfunction in multiple sclerosis: the role of orexin-A and calpain-2 - a pilot study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
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  11. Orexinergic System in Neurodegenerative Diseases.Frontiers in aging neuroscience · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Mehmet GencerDepartment of Neurology, Haydarpasa Numune Education and Research Hospital, Istanbul University, Istanbul, Turkey.
Ece AkbayırDepartment of Neuroscience, Aziz Sancar Institute of Experimental Medical Research, Istanbul University, Istanbul, Turkey.
Melis ŞenDepartment of Neuroscience, Aziz Sancar Institute of Experimental Medical Research, Istanbul University, Istanbul, Turkey.
Erdil ArsoyDepartment of Neurology, Haydarpasa Numune Education and Research Hospital, Istanbul University, Istanbul, Turkey.
Vuslat YılmazDepartment of Neuroscience, Aziz Sancar Institute of Experimental Medical Research, Istanbul University, Istanbul, Turkey.
Nesrin BulutDepartment of Neurology, Haydarpasa Numune Education and Research Hospital, Istanbul University, Istanbul, Turkey.
Erdem TüzünDepartment of Neuroscience, Aziz Sancar Institute of Experimental Medical Research, Istanbul University, Istanbul, Turkey. drerdem@yahoo.com.ORCID http://orcid.org/0000-0002-4483-0394
Recai TürkoğluDepartment of Neurology, Haydarpasa Numune Education and Research Hospital, Istanbul University, Istanbul, Turkey.
Haydarpaşa Numune Eğitim ve Araştırma Hastanesi · TRIstanbul University · TRHUN-REN Institute of Experimental Medicine · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDiencephalon is frequently affected in multiple sclerosis (MS), and lesions of this region are associated with increased disability. Orexin-A and melatonin, two foremost mediators of diencephalon, modulate cognitive and motor functions through several pathways including the brain-derived neurotrophic factor (BDNF)-cAMP response element-binding protein (CREB) signaling pathway. In this pilot study, our aim was to investigate the prognostic value of these factors in progression of cognitive and physical disability.

methodsLevels of BDNF, melatonin, CREB, and orexin-A were determined by ELISA in sera of 25 relapsing remitting MS (RRMS) patients, 15 secondary progressive MS (SPMS) patients, and 20 healthy controls. Cognitive and motor functions were assessed by a neuropsychological test battery, timed 25-ft walk (T25-FW) and 9-hole peg (9-HP) tests.

resultsMS patients had significantly lower serum levels of orexin-A and BDNF than healthy controls, and SPMS patients had significantly lower levels of melatonin and orexin-A than RRMS patients. Serum orexin-A levels were negatively correlated with 9-HP, T25-FW test scores, and progression index in RRMS patients. BDNF, CREB, and melatonin levels did not show any significant correlation with clinical features including EDSS and cognitive/motor performance of the patients.

conclusionOur results suggest that orexin-A levels are decreased in parallel to disease progression and motor system deterioration in the earlier stages of the disease. Thus, orexin-A might be used as a potential biomarker of physical disability.

Indexed as

AdultBiomarkersCohort StudiesDisability EvaluationDisease ProgressionFemaleHumansMaleMiddle AgedMovement DisordersMultiple Sclerosis, Chronic ProgressiveMultiple Sclerosis, Relapsing-RemittingNeuropsychological TestsOrexinsPilot ProjectsBiomarkersOrexinsCognitiveDisabilityMelatoninMultiple sclerosisOrexin

Identifiers

PMID30645749
OpenAlexW2910380043

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.